Home › NCT07001267

Prospective Randomized Observer Blinded Single Center Study Comparing 90-day Functional Outcome in Patients Who Received Intravenous Propofol Infusion Versus Inhalational Sevoflurane for General Anesthesia During Mechanical Thrombectomy in Patients Who Suffered From Acute Ischemic Stroke

Who can join

Ages 18 and older · All sexes

Inclusion Criteria:

* \>18 years Acute ischemic stroke requiring endovascular treatment.

Exclusion Criteria:

* \<18 years
* Pregnant patients
* Patients with malignant hyperthermia
* Allergies or any contraindications to either inhalational or intravenous agents
* Patients already on intravenous anesthetic infusions
* Prisoners
* Students and employees

About the study

This study is being done to compare outcomes after surgery for individuals who receive anesthesia through by inhaling medication and individuals who receive anesthesia intravenously by needle when experiencing treatment for their stroke. Currently very little is known about the outcomes for patients when comparing these two techniques of providing anesthesia during surgery. This study will provide information regarding outcomes that will help health care providers decide which technique will be better for patients

What is being tested

• Anesthesia drugs during the surgery (procedure)

Sponsor: University of Kansas Medical Center · Participants: 120 · Started: Jun 4, 2025

Contact the study team

• Arun George, MD · Phone: 913-588-6670

Official record on ClinicalTrials.gov — NCT07001267

Locations in the U.S.

From ClinicalTrials.gov, data retrieved Sep 30, 2026. Each study sets its own eligibility; the study team decides who can join.